Evidence map›Paper›PMID 38236641›Full record

ArticleJCI insight2024

Toxin-neutralizing Abs are associated with improved T cell function following recovery from Staphylococcus aureus infection.

Maureen Kleinhenz, Zhaotao Li, Usha Chidella, Walissa Picard, Amber Wolfe, Jill Popelka, Robin Alexander, Christopher P Montgomery

Open access · goldAbstract read
In one paragraph

Article in JCI insight, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 20% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 1 synthesis or guideline pooled it, 4 citations in OpenAlex.

  1. Research progress on T-cell responses inFrontiers in microbiology · 2026
    Pooled it
  2. Article
  3. Article
  4. Review
  5. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 3 institutions in 1 country.

Maureen KleinhenzCenter for Microbial Pathogenesis, Abigail Wexner Research Institute.
Zhaotao LiCenter for Microbial Pathogenesis, Abigail Wexner Research Institute.
Usha ChidellaCenter for Microbial Pathogenesis, Abigail Wexner Research Institute.
Walissa PicardCenter for Microbial Pathogenesis, Abigail Wexner Research Institute.
Amber WolfeDivision of Critical Care Medicine; and.
Jill PopelkaDivision of Critical Care Medicine; and.
Robin AlexanderBiostatistics Resource, Nationwide Children's Hospital, Columbus, Ohio, USA.
Christopher P MontgomeryCenter for Microbial Pathogenesis, Abigail Wexner Research Institute.
Nationwide Children's Hospital · USSociety of Critical Care Medicine · USThe Ohio State University · US

Funding

Overcoming pathogen-mediated immune evasion: a translational approach to pediatric Staphylococcus aureus vaccine development - Resubmission 01R01AI125489 · NIAID · RESEARCH INST NATIONWIDE CHILDREN'S HOSP · PI MONTGOMERY, CHRISTOPHER · 2017 to 2020
$1.5M
NIAID NIH HHS R01 AI125489
6 · The paper itself

Abstract

BACKGROUNDT cell responses are impaired in Staphylococcus aureus-infected children, highlighting a potential mechanism of immune evasion. This study tested the hypotheses that toxin-specific antibodies protect immune cells from bacterial killing and are associated with improved T cell function following infection.METHODSS. aureus-infected and healthy children (N = 33 each) were prospectively enrolled. During acute infection and convalescence, we quantified toxin-specific IgG levels by ELISA, antibody function using a cell killing assay, and functional T cell responses by ELISPOT.RESULTSThere were no differences in toxin-specific IgG levels or ability to neutralize toxin-mediated immune cell killing between healthy and acutely infected children, but antibody levels and function increased following infection. Similarly, T cell function, which was impaired during acute infection, improved following infection. However, the response to infection was highly variable; up to half of children did not have improved antibody or T cell function. Serum from children with higher α-hemolysin-specific IgG levels more strongly protected immune cells against toxin-mediated killing. Importantly, children whose serum more strongly protected against toxin-mediated killing also had stronger immune responses to infection, characterized by more elicited antibodies and greater improvement in T cell function following infection.CONCLUSIONThis study demonstrates that, despite T cell impairment during acute infection, S. aureus elicits toxin-neutralizing antibodies. Individual antibody responses and T cell recovery are variable. These findings also suggest that toxin-neutralizing antibodies protect antigen-presenting cells and T cells, thereby promoting immune recovery. Finally, failure to elicit toxin-neutralizing antibodies may identify children at risk for prolonged T cell suppression.FUNDINGNIH National Institute of Allergy and Infectious Diseases R01AI125489 and Nationwide Children's Hospital.

Indexed as

Bacterial ToxinsStaphylococcal InfectionsAntibodies, BacterialAntibodies, NeutralizingChildHumansImmunoglobulin GStaphylococcus aureusT-LymphocytesAntibodies, BacterialAntibodies, NeutralizingBacterial ToxinsImmunoglobulin GAdaptive immunityBacterial infectionsImmunologyInfectious diseaseT cells

Identifiers

PMID38236641
PMCPMC11143924
OpenAlexW4390986081

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.